BOWIE, Md., April 14, 2025 (GLOBE NEWSWIRE) -- The 118 undersigned organizations - representing people living with epilepsy; caregivers and loved ones; physicians, care providers, and epilepsy centers; epilepsy researchers; and others - are united in opposition to recent actions by the Administration and Congress to cut vital federal epilepsy programs. As the fourth most common neurological condition in the world and with nearly 3.4 million Americans living with active epilepsy, we must be doing more - not less - to understand and treat epilepsy, develop cures, improve the quality of life for people with epilepsy, and increase public awareness. We urge policymakers to reverse these cuts and ensure that fundamental epilepsy public health and research programs are maintained:

  • Centers for Disease Control and Prevention (CDC)'s Epilepsy Program: At the beginning of April, Reductions in Force (RIF) notices were issued to staff within the CDC's National Center for Chronic Disease Prevention and Health Promotion Epilepsy Program. The CDC Epilepsy Program is the only public health program related explicitly to epilepsy with a national scope and community programs that examine, test, and share strategies to improve the lives of people with epilepsy and their loved ones. This critical program supports seizure recognition and first aid training, including for school personnel; research to better understand the burden and risk factors of epilepsy; self-management programs that improve the health and well-being of people with epilepsy; and Project ECHO so that epilepsy specialists can help primary care doctors in rural communities.
  • Congressionally Directed Medical Research Programs (CDMRP): In its final FY25 funding bill, Congress cut appropriations for the Congressionally Directed Medical Research Program (CDMRP) by 57%. This has completely eliminated specific funding for research related to Tuberous Sclerosis Complex (TSC), post-traumatic epilepsy, and traumatic brain injury (TBI) and psychological health. The elimination of this funding will have harmful impacts and set back innovation. TBI is a leading and significant form of injury in service people, especially those in combat and training environments, and it can lead to post-traumatic epilepsy for 50% of those with severe TBI. For many years, these research programs have funded cutting-edge research to better understand and address these neurologic conditions that can affect Service Members, Veterans, and their families. These cuts must be restored to continue progress in epilepsy research.
  • National Institutes of Health (NIH) and National Institute of Neurological Disorders and Stroke (NINDS): Within NIH, several institutes fund epilepsy-related research which has helped better understand, diagnose, and treat epilepsy-most notably, the National Institute of Neurological Disorders and Stroke (NINDS). In the past several weeks, nearly 20% of the NINDS staff have been impacted by RIFs, including people dedicated to epilepsy. Beyond a loss of expertise, we also understand that there will be significant cuts to both funding opportunities and contracts. We are extremely concerned about the impact of these cuts on current and future epilepsy research activities and know they are impeding our shared goal of curing epilepsy.
  • Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC): The ACHDNC was also terminated in early April. For more than 20 years, this committee has governed the Recommended Uniform Screening Panel (RUSP), which helps to ensure that newborns have access to screening, diagnosis, and intervention for serious medical conditions. Some conditions on the RUSP list can cause seizures and there are many other rare disorders that cause seizures and epilepsy in infants and children that could be added. We are extremely concerned about the impact the dissolution of the ACHDNC will have on infants, children, and their caregivers in the rare epilepsy community. The dissolution of this committee completely terminates any possibility of enhancement, expansion, and improvement of the US's ability to reduce preventable suffering and deaths of infants. We urge that it be reinstated as soon as possible.

These actions will halt progress in preventing, diagnosing, treating, curing, and managing epilepsy. These changes are happening at a time when many other significant threats are looming for people with epilepsy and their families, including possible cuts to Medicaid and the possible dismantling of the U.S. Department of Education. About 40% of people with epilepsy rely on Medicaid for access to healthcare and long-term services and supports. Meanwhile, the U.S. Department of Education is vital to ensuring that the rights of students with disabilities are protected and enforced.  

Epilepsy looks different for each person. There are many types of seizures and syndromes, and epilepsy affects people throughout their lifespan with varied causes and associated conditions. Most importantly, delayed recognition and inadequate treatment increases a person's risk of seizures, brain damage, disability, and death. Epilepsy and/or seizures impose an annual economic healthcare burden of $54 billion in the U.S. This is why epilepsy research and programs are so critical to the public health and economic health of our nation.

The epilepsy community is devastated by these cuts, and we need action now. We call on policymakers to restore funding and staffing for these vital programs. Please contact Laura Weidner, Chief Advocacy and Government Relations Officer for the Epilepsy Foundation at lweidner@efa.org or Johanna Gray, Deputy Director of the National Association of Epilepsy Centers at jgray@artemispolicygroup.com with any questions.

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National and International Organizations

AHC Foundation

American Epilepsy Society

Angelman Syndrome Foundation

Angels of Epilepsy, Inc.

Autism Faith Network

CACNA1A Foundation

Child Neurology Foundation

Coalition to Cure CHD2

COMBINEDBrain Inc.

CSNK2B Foundation

CURE Epilepsy

Cure KCNH1 Foundation

CureSHANK

Danny Did Foundation

Developmental and Epileptic Encephalopathies Project (DEE-P Connections)

DLG4 SHINE Foundation

Doose Syndrome Epilepsy Alliance

Dravet Syndrome Foundation

Dup15q Alliance

Epilepsies Action Network (EAN)

Epilepsy Alliance America

Epilepsy Foundation of America

Epilepsy Information Service, Wake Forest School of Medicine

Epilepsy Wellness Advocates

FamilieSCN2A Foundation

Foundation for Angelman Syndrome Therapeutics

GABA-A Alliance

GNB1 Advocacy Group, Inc.

GRIN2B Foundation

Hidden Truths Project

Hope for HIE

Hope for ULD

International Foundation for CDKL5 Research

International League Against Epilepsy - North America

International SCN8A Alliance

Joanna Sophia Foundation

KCNQ2 Cure Alliance

KPTN Alliance

Lightning and Love Foundation

National Association of Epilepsy Centers

NORSE Institute

Partners Against Mortality in Epilepsy (PAME)

Pediatric Epilepsy Research Consortium

Pediatric Epilepsy Surgery Alliance

Phelan-McDermid Syndrome Foundation

Rare Epilepsy Network (REN) Coordinating Committee

Ring14 USA

Ring20USA

Schinzel-Giedion Syndrome Foundation

STXBP1 Foundation

Tatton Brown Rahman Syndrome Community

TESS Research Foundation

The Cute Syndrome Foundation

The Mark Shaparin Foundation

The Rory Belle Foundation

TSC Alliance

v-ATPase Alliance

State and Local Organizations

Beta Spectrin Foundation

Empowering People's Independence

EPIC LI/Epilepsy Foundation Long Island

Epilepsy Advocacy Network

Epilepsy Alliance Louisiana

Epilepsy Alliance North Carolina

Epilepsy Foundation Alabama

Epilepsy Foundation Alaska

Epilepsy Foundation Arizona

Epilepsy Foundation Arkansas

Epilepsy Foundation Central & South Texas

Epilepsy Foundation Eastern PA

Epilepsy Foundation Florida

Epilepsy Foundation Greater Orange County

Epilepsy Foundation Indiana

Epilepsy Foundation Iowa

Epilepsy Foundation Los Angeles

Epilepsy Foundation Louisiana

Epilepsy Foundation Maryland

Epilepsy Foundation Maryland Chapter

Epilepsy Foundation Metro D.C.

Epilepsy Foundation Mississippi

Epilepsy Foundation Montana

Epilepsy Foundation Nebraska

Epilepsy Foundation Nevada

Epilepsy Foundation New England

Epilepsy Foundation New Jersey

Epilepsy Foundation New Mexico

Epilepsy Foundation North Carolina

Epilepsy Foundation North Dakota

Epilepsy Foundation of Connecticut

Epilepsy Foundation of Delaware

Epilepsy Foundation of Greater Chicago

Epilepsy Foundation of Idaho

Epilepsy Foundation of Kentuckiana

Epilepsy Foundation of Michigan

Epilepsy Foundation of Minnesota

Epilepsy Foundation of Missouri and Kansas

Epilepsy Foundation of Northern California

Epilepsy Foundation of Northeastern New York

Epilepsy Foundation of San Diego County

Epilepsy Foundation of Southeast Tennessee

Epilepsy Foundation of Virginia

Epilepsy Foundation of Wisconsin

Epilepsy Foundation Ohio

Epilepsy Foundation Oklahoma

Epilepsy Foundation Oregon

Epilepsy Foundation South Carolina

Epilepsy Foundation South Dakota

Epilepsy Foundation Texas

Epilepsy Foundation Utah

Epilepsy Foundation Washington

Epilepsy Foundation West Virginia

Epilepsy Services of New Jersey

Epitome of Epilepsy nonprofit organization

HardyHandz Foundation

Joey's Song

Rea of Hope for a Cure Foundation

Sociedad Puertorriqueña de Epilepsia

South Carolina Advocates For Epilepsy

The Epilepsy Institute DBA the Epilepsy Foundation of Metro NY